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A Case of Neurogenic Shock from Intussuception Secondary to a Small Bowel Lipoma

Kim SH, Ko KO, Lee YH

  • KMID: 2329524
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):220-224.
For neurologic symptoms such as mental changes, the etiologies should be thoroughly looked for. Neurologic problems are primarily assessed by medical history, physical and neurologic examination, electroencephalogram, neuroimaging studies. Furthermore,...
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Prolonged Survival of an Adult with Hydranencephaly

Bae JS, Kim SJ, Park KM, Chi GH, Hwang TG

  • KMID: 2329523
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):216-219.
Hydranencephaly is a rare condition in which the brain's cerebral hemispheres are absent and replaced by sacs filled with cerebrospinal fluid. The prognosis for children with hydranencephaly is generally poor,...
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A Case of Child with Miller Fisher Syndrome Diagnosed by Anti-GQ1b Antibody from Mycoplasma Pneumoniae

Chueh H, Kwon EY, Shin HY, Hwang KG

  • KMID: 2329522
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):211-215.
Miller Fisher syndrome, first reported by Miller Fisher in 1956, is characterized by a triad of external ophthalmoplegia, areflexia, and ataxia. Many features shared with Guillain-Barre syndrome; CSF usually shows...
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Two Cases of Miller Fisher Syndrome without Ataxia

Ju M, Lee KH, Kim SY

  • KMID: 2329521
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):205-210.
A classic triad of acute external ophthalmoplegia, areflexia and ataxia characterizes Miller Fisher syndrome(MFS). Diagnosis is based on clinical findings and supported by two laboratory findings; CSF albuminocytological dissociation and...
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A Case of Menkes disease with Infantile Spasm

Ahn SH, Park SY, Kang SG, Lee JE, Kwon YS, Son BK, Yoo HW

  • KMID: 2329520
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):199-204.
Menkes disease, so called kinky-hair syndrome, is a rare, genetic and progressive neurodegenerative disorder. It is caused by a mutation in the ATP7A gene, which codes for the copper transporting...
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A Case of PEHO Syndrome

Moon HK

  • KMID: 2329519
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):192-198.
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy(PEHO) syndrome was first described in 1991 by Salonen. It is a rare, autosomal recessive, and severe neurodegenerative disease with onset in early...
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Characteristics of Sleep Disorders in Childhood and Adolescence

Yoon JM, Lee HR, Lee KH

  • KMID: 2329518
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):185-191.
PURPOSE: Sleep disorders are common diseases in childhood and adolescence. Daytime sleepiness, fatigue, headache, etc caused by sleep disorders may affect daily activities and school performance. Authors conducted this study...
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Moyamoya Disease in Children and Adolescents

Lee SI, Chi GH, Hwang TG

  • KMID: 2329517
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):179-184.
PURPOSE: Moyamoya disease is a chronic cerebrovascular illness characterized by bilateral stenoses or occlusions of the arteries around the circle of Willis with prominent collateral circulation. We studied 36 children...
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Clinical Features of Moyamoya Disease in Children

Yang WS, Oh EY, Lee GY, Jeong DC, Kim YH, Lee IG, Chung SY, Hwang HS

  • KMID: 2329516
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):170-178.
PURPOSE: Moyamoya disease, is a chronic progressive cerebrovascular occlusive disorder that can lead to permanent neurologic deficit. The aim of this study is to analyze clinical features, radiologic findings, and...
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Prognostic Value of Electrophysiologic Tests in Children with Facial Nerve Palsy

Hong EH, Kim JM, Kwon SH

  • KMID: 2329515
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):162-169.
PURPOSE: This study was aimed to evaluate the value of electrophysiologic tests for determining prognosis in children with facial nerve palsy. METHODS: We retrospectively analyzed 37 children diagnosed as the facial...
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Multimodal Management of Lennox-Gastaut Syndrome

Yum MS, Hong SH, Lee JK, You SJ, Kim DS, Ko TS

  • KMID: 2329514
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):154-161.
PURPOSE: Lennox-Gastaut syndrome(LGS) is a childhood epileptic encephalopathy characterized by an electroclinical triad of generalized slow spike and wave activities in the EEG, multiple types of epileptic seizures, and slow...
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Single Nucleotide Polymorphisms of GABRG2 in Idiopathic Generalized Epilepsies(IGEs)

Yeon YH, Seung SJ, Hwang HS, Kim E, Kim YH, Lee IG, Chung SY

  • KMID: 2329513
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):148-153.
PURPOSE: Mutations in gamma-aminobutyric acid(GABA) A receptor gamma2 subunit gene (GABRG2) were independently identified in families of generalized epilepsy with febrile seizures plus(GEFS+) and families of absence epilepsy and febrile...
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Introduction of National Health Screening Program for Infant and Children

Eun BL, Kim SW, Kim YK, Kim JW, Moon JS, Park SK, Sung IK, Shin SM, Yoo SM, Eun SH, Lee HK, Lim HT, Chung HJ

  • KMID: 2329512
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):142-147.
No abstract available.
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Glucose Transporter Type 1 Deficiency Syndrome

Kim SK

  • KMID: 2329511
  • J Korean Child Neurol Soc.
  • 2007 Nov;15(2):131-141.
D-glucose is an essential fuel for metabolism in mammalian cells and the predominant fuel source for the brain. Transport of glucose across tissue barriers is mediated by stereospecific transporter proteins....
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